Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1326123837
rs1326123837
2 0.925 0.040 11 119025310 missense variant C/T snv 7.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs193302889
rs193302889
3 0.882 0.120 11 119029289 missense variant A/T snv 8.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs782692832
rs782692832
2 0.925 0.040 11 119026688 missense variant C/T snv 4.6E-06 0.010 1.000 1 2020 2020